TMR+ Bowtie Baseplate Reamer
- Primary DI
- 00889024644946
- Brand
- TMR+ Bowtie Baseplate Reamer
- Company
- Zimmer, Inc.
- Model
- SSI006761
- Catalog number
- SSI006761
- Published
- 2022-05-06
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HSD | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented | Orthopedic | 2 |
| KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| KWT | Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
| PHX | Shoulder Prosthesis, Reverse Configuration | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K172767 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00889024644946 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00889024644946 | 00889024644946 | 889024644946 | 0889024644946 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic reamer guide | An orthopaedic surgical device that functions as a guide for an orthopaedic reamer. The guide, commonly called a spigot, is inserted into a predetermined site where bone is to be resected for the acceptance of a prosthetic implant, typically at or within a joint (e.g., the condyle head of the knee, the olecranon of the ulna) or for the reaming of the intramedullary canal for acceptance of an intramedullary nail. The device allows the controlled cutting action of the reamer which is steered down its length. It is typically made of a high-grade stainless steel alloy; it comes in varying sizes. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 1 (800) 343-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 056038268
- Device count
- 1
- Serial number
- true
- Sterilization required before use
- true
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